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Senzime receives FDA 510k-clearance

Pia Renaudin CEO Senzime
The company’s TetraGraph-system has now received FDA 510k-clearance for use in children with the disposable sensor TetraSens Pediatric. Senzime can thus broaden the indication for TetraGraph to also monitor infants and young children who have received muscle paralyzing drugs as part of anesthes
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